Design Quality Engineer

Philips International; Pune District; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Philips, a health technology company, seeks a Design Quality Engineer to support quality, reliability and safety across the lifecycle of medical devices. You will act as a product quality lead, interfacing with regulatory affairs and cross-functional teams to ensure customer-focused quality outcomes.

Responsibilities include establishing quality strategies, leading quality plans, and driving improvements through post-market data and RCA. Strong English communication is required.

Qualifications

• Validates key design inputs like usability, reliability, performance, and safety.
• Experience with quality planning and lifecycle processes.
• ASQ CQE or CQM certifications preferred; 13485 auditor preferred.

Responsibilities

• Establish quality and reliability strategy for the product(s) in scope.
• Define activities in the Product Quality Plan to meet targets.
• Review reliability plans and key quality requirements; ensure transfer to manufacturing and supply chain.
• Lead root cause analysis and problem solving for design quality issues.
• Support field and post-market data to improve design quality across lifecycle.

Skills

Usability validation

Reliability analysis

Root cause analysis

Quality planning

Education

Bachelors in Mechanical Engineering / Electronics / Science

Masters in engineering/science (optional)

Job description

Job Title Design Quality Engineer Job Description

Job title: Design Quality Engineer

You Role

While positioned within the Business Unit MR, reporting to the Segment OEM & Coils DQE Leader, you will support the Quality, Reliability and Safety of Medical Devices though all lifecycle phases of the medical device. You will contribute to achieve quality objectives as they relate to: Customer Experience, Complaint Rate, and First Past Yield. You will work in an independent Quality & Regulatory organization with key stakeholders during various stages of the design, development and maintenance of the medical device. Representing Design Quality during the execution of new development programs and sustaining activities and interfacing with regulatory affairs Independent oversight of product performance as this relates to Product Quality, Safety and Reliability

During (early) Development and Lifecycle Maintenance

• Participate in establishing the quality and reliability strategy specific to the product(s) in scope.


• Involved in quality target setting in Project Charter


• Act as a product quality lead by defining the activities in the Product Quality Plan to meet product quality targets


• Contribute to the execution and delivery of results specific to product quality: Review reliability plans , review key quality related requirements , ensure a proper transfer of design specifications to manufacturing and supply chain and service, perform assessment on the design/architecture on suitability for the quality criteria, and review key product related deliverables (Reliability Reports, Reliability modelling for predictive analysis, FMEA’s, Change Point Analysis, etc.)


• Apply and facilitate Design for Quality & Reliability best practices (FMEAs, robust design, V&V, root cause analysis & problem solving)


• Regularly go through the history of quality issues (leverage data of post-market analysis like Complaints, Quality Notifications, DeFOA, Defect) and drive improvement through proposals


• Support and lead quality related problem solving and root cause analysis as they relate to design and development and define and establish best practices

Your KAR's

• Ensures that the Voice of the Patient/Consumer is adequately represented in the project team ensuring patient/consumer safety and quality in decision making, e.g. setting of unambiguous appropriate customer/patient-focused targets (reliability, usability, availability, serviceability, manufacturability)


• Is single point of contact in project teams for end-to-end design quality, collaborating with multiple stakeholders within and outside of quality function, responsible to provide direction on design quality-related matters where needed


• In partnership with other functions, defines and manages the wholistic patient/consumer safety, quality and reliability strategy and approach, overseeing execution and quality of results, driving to sufficient confidence in the product/service prior to release to market


• Is responsible for appropriate and actionable quality plans (as part of Project Management Plan and/or separate) that include all phases of the project, and provides effective insight and oversight of the execution of the Quality Plan(s), Risk Management activities, in accordance with QMS processes


• In partnership with other functions, is responsible for delivery of patient/consumer safety, quality and compliance in key design input traceable to key design output, in accordance with applicable QMS processes


• Supports and drives the use of focused methodologies, e.g. Design for Reliability, Design for Six Sigma, RCA, etc, to support the quality objectives.


• Ensures patient/consumer safety & quality in Design Reviews, FMEA and Safety Risk Management, including CTS/CTQ attribute usage, and Verification & Validation with appropriate statistical confidence and reliability.


• Assesses patient/consumer safety & quality performance throughout all phases of the project and post-launch product quality analysis during the monitoring phase, reporting (with sufficient objectiveness and coverage) at the project gates.


• Feeds back patient/consumer safety & quality related post-market data in applicable product development & maintenance processes.


• Supports proper root cause investigation of patient/consumer safety and quality-related issues in a cross-functional approach, driving corrective actions to prevent recurrence

You're the right fit if

• Experience: 5+ years of industry experience, must have experience in Healthcare/Medical device industry.


• Skills: Validates key design inputs like usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability, and costs. Applied IA knowledge is a pre.


• Education: Bachelor's Degree/Master's Degree in Mechanical Engineering, Electronics Engineering, Science, or equivalent.


• Certifications: ASQ CQE or CQM preferred. 13485 auditor preferred.


• High-level English language proficiency including strong writing skills.

How we work together

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. Indicate if this role is an office/field/onsite role.

About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won\'t stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. Learn more about our business. Discover our rich and exciting history. Learn more about our purpose.

In more than 130 years, we have been creating technologies and innovations that improve people\'s lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health. Together, we deliver better care for more people because we believe that every human matters.

When people feel cared for and listened to, they bring their best qualities to work, leading to better collaboration, communication, innovation and success. It is the policy of Philips to provide equal employment and advancement opportunities to all qualified employees and applicants for employment without regard to race, color, religion, sex, pregnancy/childbirth or related medical conditions, age, ethnic or national origin, sexual orientation, gender identity or expression, physical or mental disability, genetic information, citizenship status, veteran or military status, marital or domestic partner status or any other characteristic protected by law.

To ensure reasonable accommodations for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans\' Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact 888-367-7223, option 5, for assistance.

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